Primary Site >> Liver Cancer
Gene >> ADAM12
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368679 |
| Start | 126064991:126064991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1433C>T |
| AA Mutation | p.Ala478Val(p.A478V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368679 |
| Start | 126108624:126108624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.719G>A |
| AA Mutation | p.Arg240Gln(p.R240Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000368679 |
| Start | 126071477:126071477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1332G>T |
| AA Mutation | p.Glu444Asp(p.E444D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368679 |
| Start | 126064866:126064866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1558T>C |
| AA Mutation | p.Tyr520His(p.Y520H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368679 |
| Start | 126071585:126071585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1224G>A |
| AA Mutation | p.Met408Ile(p.M408I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368679 |
| Start | 126109809:126109809(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.644A>G |
| AA Mutation | p.Tyr215Cys(p.Y215C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368679 |
| Start | 126135641:126135641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751757189 |
| CDS Mutation | c.368G>A |
| AA Mutation | p.Gly123Glu(p.G123E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000368679 |
| Start | 126019803:126019803(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2561delC |
| AA Mutation | p.Pro854LeufsTer85(p.P854Lfs*85) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000368679 |
| Start | 126071476:126071476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1332+1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000368679 |
| Start | 126118036:126118036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.612+2T>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000368679 |
| Start | 126065002:126065002(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1423-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |